TY - JOUR
T1 - Concomitant augmentation of type 1 CD4+ and CD8+ T-cell responses during successful interferon-α and ribavirin treatment for chronic hepatitis C virus infection
AU - Sreenarasimhaiah, Jayaprakash
AU - Jaramillo, Andrés
AU - Crippin, Jeffrey
AU - Lisker-Melman, Mauricio
AU - Chapman, William C.
AU - Mohanakumar, T.
N1 - Funding Information:
This study was supported by the National Institute of Health Grant No. DK07130-27.
PY - 2003/5/1
Y1 - 2003/5/1
N2 - The combined interferon-α (IFN-α) and ribavirin (IFN-α/ribavirin) therapy for chronic hepatitis C virus (HCV) infection results in sustained viral eradication in 31%-64% of the patients. Previous studies have strongly suggested that HCV-specific T-cell responses maybe modulated during this therapy. The objective of this study was to further define the effect of IFN-α/ ribavirin therapy on type 1 and type 2 HCV-specific CD4+ and CD8+ T-cell responses during IFN-α/ribavirin therapy. Toward this, serial CD8+ T-cell responses to HCV-derived epitopes and CD4+ T-cell responses to the HCV core antigen were analyzed in four patients before (baseline), during (at 24 weeks), and at the end (at 48 weeks) of IFN-α/ribavirin therapy. Therapy-induced viral clearance in three patients was associated with a significant augmentation of HCV-specific type 1 CD4+ and CD8+ T-cell responses. In contrast, in a patient who did not respond to therapy, a significant HCV-specific CD4+ Th2 cell reactivity was observed accompanied by a lack of augmentation of the HCV-specific CD8+ T-cell reactivity. These results indicate that enhancement of HCV-specific CD4+ and CD8+ T-cell responses is an important factor in determining the response to the IFN-α/ribavirin therapy and the outcome of the HCV infection.
AB - The combined interferon-α (IFN-α) and ribavirin (IFN-α/ribavirin) therapy for chronic hepatitis C virus (HCV) infection results in sustained viral eradication in 31%-64% of the patients. Previous studies have strongly suggested that HCV-specific T-cell responses maybe modulated during this therapy. The objective of this study was to further define the effect of IFN-α/ ribavirin therapy on type 1 and type 2 HCV-specific CD4+ and CD8+ T-cell responses during IFN-α/ribavirin therapy. Toward this, serial CD8+ T-cell responses to HCV-derived epitopes and CD4+ T-cell responses to the HCV core antigen were analyzed in four patients before (baseline), during (at 24 weeks), and at the end (at 48 weeks) of IFN-α/ribavirin therapy. Therapy-induced viral clearance in three patients was associated with a significant augmentation of HCV-specific type 1 CD4+ and CD8+ T-cell responses. In contrast, in a patient who did not respond to therapy, a significant HCV-specific CD4+ Th2 cell reactivity was observed accompanied by a lack of augmentation of the HCV-specific CD8+ T-cell reactivity. These results indicate that enhancement of HCV-specific CD4+ and CD8+ T-cell responses is an important factor in determining the response to the IFN-α/ribavirin therapy and the outcome of the HCV infection.
KW - CD4 T cells
KW - CD8 T cells
KW - Hepatitis C virus
KW - IFN-α/ribavirin therapy
UR - http://www.scopus.com/inward/record.url?scp=0242515870&partnerID=8YFLogxK
U2 - 10.1016/S0198-8859(03)00041-7
DO - 10.1016/S0198-8859(03)00041-7
M3 - Article
C2 - 12691700
AN - SCOPUS:0242515870
SN - 0198-8859
VL - 64
SP - 497
EP - 504
JO - Human Immunology
JF - Human Immunology
IS - 5
ER -